Musculoskeletal/Articular Dysfunction Flashcards

1
Q

When to suspect child abuse?

A
  • Most inflicted fractures occur in infancy/early childhood.
  • Stated history not consistent with injury pattern
  • Injury inconsistent with developmental stage
  • Discrepancy and/or conflicts in caregiver stories
  • Presence of multiple fractures
  • Spiral or rib fractures in infant
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2
Q

Describe spiral fractures or rib fractures in infants.

A
  • Skeletal Survey done to detect other fractures
  • Nurses are mandatory reporters!
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3
Q

Care for a child in a cast?

A
  • Purpose: immobilization to promote healing and proper alignment
  • Neurovascular assessment (5 P’s: pain, pulse, pallor, paresthesia, paralysis)
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4
Q

Education on cast?

A

Do not put anything into the cast

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5
Q

What to assess for in a child with a cast?

A
  • assess for adequate nerve function & blood circulation in order to detect signs/symptoms of potential complications like compartment syndrome
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6
Q

What is Acute Compartment Syndrome?

A
  • serious and life-threatening complication
    • requires immediate action
    • may cause permanent damage to extremity
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7
Q

Acute compartment syndrome symptoms?

A
  • Swelling of extremity
  • Decrease or loss of pulses
  • Cool to touch
  • Extremity pale or cyanotic
  • Numbness or tingling
  • Extreme pain not controlled by medication
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8
Q

Acute compartment syndrome management?

A

Surgery (Fasciotomy) to reduce the pressure and restore circulation.

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9
Q

Child in traction purpose?

A
  • Maintains straight alignment of fractured bone
  • Decreases pain and spasms

child is laying down with legs straight in the air (90 degrees) held by string (on bandages and tape) and creates a gentle pull via a pulley and weight system

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10
Q

Child in traction nursing management?

A
  • Do not remove, adjust, or add weights unless there is a provider order.
  • Allow weights to hang freely
  • Monitor skin for redness and signs of breakdown
  • Neurovascular assessment (5 P’s)
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11
Q

What is scoliosis?

A
  • Abnormal lateral curvature of the spine
  • Generally noticeable after preadolescent growth spurt
  • Asymmetry of shoulder height, scapular or flank shape, or hip height
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12
Q

Scoliosis treatment?

A

Exercise, bracing, and/or surgery

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13
Q

What is Developmental Dysplasia of the Hip (DDH)?

A

Abnormal development of the hip joint during fetal growth or early infancy.

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14
Q

Signs of Developmental Dysplasia of the Hip (DDH)?

A

The socket of the hip (acetabulum) is too shallow and the femoral head is not held tightly in place, so the hip joint is loose.

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15
Q

Developmental Dysplasia of the Hip (DDH) Treatment?

A
  • Pavlik Harness (0-6 mo)
  • Spica cast (6-24 mo)
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16
Q

Nursing care management Developmental Dysplasia of Hip (DDH)?

A
  • Assessment of skin integrity
  • Education and support of family
  • Promotion of normal growth and development
17
Q

What is Legg-Calvé-Perthes Disease?

A
  • Idiopathic temporary disruption of blood to femoral head (avascular necrosis)
    • Poor blood supply → weakened bone → gradually breaks apart and can potentially lose its round shape
  • Occurs in children 3 to 12 years of age (peak incidence 5-8)
18
Q

Legg-Calvé-Perthes Disease symptoms?

A
  • gradual onset
  • limping
  • hip pain
19
Q

Legg-Calvé-Perthes Disease diagnostic studies?

A

MRI

20
Q

Legg-Calvé-Perthes Disease treatment?

A

Rest (no weight) and NSAIDS

21
Q

What is Slipped Femoral Capital Epiphysis?

A
  • Spontaneous displacement of the femoral head (epiphysis) from femoral neck
  • Involves the femoral growth plate
  • Occurs between 10-16 yrs old
22
Q

Slipped Femoral Capital Epiphysis symptoms?

A
  • hip pain
  • limping
  • difficulty bearing weight on the affected leg
23
Q

Slipped Femoral Capital Epiphysis treatment?

A

Surgery

  • Screw fixation is standard care
24
Q

Osteogenesis Imperfecta (OI) manifestations?

A
  • Blue sclera
  • Fx early on in childhood
  • Short stature
  • Ligamentous laxity
25
Q

Osteogenesis Imperfecta (OI) nursing management?

A
  • Caution with handling to prevent fractures
  • PT/OT recommendations
  • Family education and support
  • Genetic counseling
26
Q

Osteogenesis Imperfecta (OI) drug management?

A
  • Drugs- bisphosphonate therapy
    • Pamidronate (Aredia)
    • Promote bone density and prevent fractures